dc.creatorTaverna Porro, Marisa Lia
dc.creatorIglesias, Luis Emilio
dc.creatorMontserrat, Javier Marcelo
dc.creatorIribarren, Adolfo Marcelo
dc.date.accessioned2019-07-17T18:04:11Z
dc.date.accessioned2022-10-15T09:36:59Z
dc.date.available2019-07-17T18:04:11Z
dc.date.available2022-10-15T09:36:59Z
dc.date.created2019-07-17T18:04:11Z
dc.date.issued2007-03
dc.identifierTaverna Porro, Marisa Lia; Iglesias, Luis Emilio; Montserrat, Javier Marcelo; Iribarren, Adolfo Marcelo; Deacetylation of furanosides using banana as biocatalyst; Elsevier Science; Journal of Molecular Catalysis B: Enzymatic; 44; 3-4; 3-2007; 138-143
dc.identifier1381-1177
dc.identifierhttp://hdl.handle.net/11336/79752
dc.identifierCONICET Digital
dc.identifierCONICET
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/4371148
dc.description.abstractThe deacylation under hydrolytic conditions of methyl 2,3,5-tri-O-acetyl-α-d-ribofuranoside, methyl 2,3,5-tri-O-acetyl-β-d-ribofuranoside, methyl 2,3,5-tri-O-acetyl-α,β-d-arabinofuranosides and alkyl 2,3,5-tri-O-acetyl-α,β-xylofuranosides have been studied using banana whole tissue as biocatalyst. Reaction regioselectivity strongly depends on substrate structure. Hydrolysis of methyl 2,3,5-tri-O-acetyl-α-d-ribofuranoside afforded methyl 2,3-di-O-acetyl-α-d-ribofuranoside in quantitative yield.
dc.languageeng
dc.publisherElsevier Science
dc.relationinfo:eu-repo/semantics/altIdentifier/url/http://www.sciencedirect.com/science/article/pii/S138111770600302X
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/https://doi.org/10.1016/j.molcatb.2006.10.001
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.subjectBANANA
dc.subjectDEPROTECTION
dc.subjectFURANOSIDES
dc.subjectHYDROLASES
dc.subjectREGIOSELECTIVE DEACETYLATION
dc.titleDeacetylation of furanosides using banana as biocatalyst
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:ar-repo/semantics/artículo
dc.typeinfo:eu-repo/semantics/publishedVersion


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